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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Comparison of Atomic Force Microscopy and Scanning Ion Conductance Microscopy for Live Cell Imaging
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Comparison of Atomic Force Microscopy and Scanning Ion Conductance Microscopy for Live Cell Imaging

机译:原子力显微镜和扫描电导显微镜在活细胞成像中的比较

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摘要

Atomic force microscopy (AFM) and scanning ion conductance microscopy (SICM) are excellent and commonly used techniques for imaging the topography of living cells with high resolution. We present a direct comparison of AFM and SICM for imaging microvilli, which are small features on the surface of living cells, and for imaging the shape of whole cells. The imaging quality on microvilli increased significantly after cell fixation for AFM, whereas for SICM it remained constant. The apparent shape of whole cells in the case of AFM depended on the imaging force, which deformed the cell. In the case of SICM, cell deformations were avoided, owing to the contact-free imaging mechanism. We estimated that the lateral resolution on living cells is limited by the cell's elastic modulus for AFM, while it is not for SICM. By long-term, time-lapse imaging of microvilli dynamics, we showed that the imaging quality decreased with time for AFM, while it remained constant for SICM.
机译:原子力显微镜(AFM)和扫描离子电导显微镜(SICM)是出色的常用技术,可对高分辨率的活细胞进行地形成像。我们提出了AFM和SICM的直接比较,用于成像微绒毛,这是活细胞表面的小特征,并且用于成像全细胞的形状。细胞固定后,AFM的微绒毛成像质量显着提高,而SICM则保持不变。在AFM的情况下,整个细胞的外观形状取决于成像力,从而使细胞变形。在SICM的情况下,由于无接触成像机制,避免了细胞变形。我们估计,活细胞的横向分辨率受AFM的细胞弹性模量的限制,而不受SICM的限制。通过微绒毛动力学的长期延时成像,我们发现AFM的成像质量随时间下降,而SICM的成像质量则保持不变。

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